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Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor
Author(s) -
Lopez Genghis H.,
McGowan Eunike C.,
Condon Jennifer A.,
Schoeman Elizna M.,
Millard Glenda M.,
O'Brien Helen,
Roulis Eileen V.,
OchoaGaray Gorka,
Liew YewWah,
Flower Robert L.,
Hyland Catherine A.
Publication year - 2017
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/trf.14250
Subject(s) - sanger sequencing , genotyping , exon , amplicon , genetics , snp genotyping , dna sequencing , gene , snp , biology , snp array , computational biology , polymerase chain reaction , genotype , single nucleotide polymorphism